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Geiz 6.02.01.G

by Bear-Ent, LLC

Geiz 6.02.01.G is a Class I device made by Bear-Ent, LLC, listed in FDA GUDID since 5 Mar 2026 (UDI-DI G04360201G0), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberG04360201G0 UDI-DI Date5 Mar 2026ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Geiz
Generic name
Ear speculum, reusable
Model / Ref / Catalog
6.02.01.G
Primary DI / UDI-DI
G04360201G0
FDA product code
EPY
GMDN term
Ear speculum, reusable
Device class
Class I
Regulation number
878.1800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Similar devices

Other devices filed under FDA product code EPY (Speculum, Ent).

Other devices from Bear-Ent, LLC

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)